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ONTOLOGY REPORT - ANNOTATIONS


Term:somatoform disorder
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Accession:DOID:4737 term browser browse the term
Definition:Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V)
Synonyms:exact_synonym: Briquet syndrome;   Pain Disorder;   Psychophysiological Disorder;   Psychophysiological Disorders;   medically unexplained syndrome;   medically unexplained syndromes;   physiological malfunction arising from mental factor;   psychophysiologic disorder;   psychophysiologic disorders;   psychosomatic disorder;   psychosomatic disorders;   somatoform disorders
 primary_id: MESH:D011602;   MESH:D013001
 xref: ICD10CM:F45;   ICD10CM:F45.9;   ICD9CM:300.8;   NCI:C34956
For additional species annotation, visit the Alliance of Genome Resources.


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somatoform disorder term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC100972354 interferon alpha-2 JBrowse link 9 21,245,017 21,246,210 RGD:9068941
body dysmorphic disorder term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CALHM4 calcium homeostasis modulator family member 4 JBrowse link 6 114,337,385 114,369,423 RGD:9068941
G CALHM5 calcium homeostasis modulator family member 5 JBrowse link 6 114,319,599 114,325,898 RGD:9068941
G CALHM6 calcium homeostasis modulator family member 6 JBrowse link 6 114,263,062 114,265,898 RGD:9068941
G COL10A1 collagen type X alpha 1 chain JBrowse link 6 113,921,538 113,961,490 RGD:9068941
G DCBLD1 discoidin, CUB and LCCL domain containing 1 JBrowse link 6 115,290,931 115,358,249 RGD:9068941
G DSE dermatan sulfate epimerase JBrowse link 6 114,173,641 114,246,129 RGD:9068941
G FAM162B family with sequence similarity 162 member B JBrowse link 6 114,534,874 114,573,958 RGD:9068941
G FRK fyn related Src family tyrosine kinase JBrowse link 6 113,748,464 113,903,350 RGD:9068941
G GOPC golgi associated PDZ and coiled-coil motif containing JBrowse link 6 115,368,682 115,411,140 RGD:9068941
G GPRC6A G protein-coupled receptor class C group 6 member A JBrowse link 6 114,601,360 114,638,286 RGD:9068941
G HDAC2 histone deacetylase 2 JBrowse link 6 111,731,139 111,761,826 RGD:9068941
G HS3ST5 heparan sulfate-glucosamine 3-sulfotransferase 5 JBrowse link 6 111,846,143 112,132,706 RGD:9068941
G KPNA5 karyopherin subunit alpha 5 JBrowse link 6 114,488,850 114,550,061 RGD:9068941
G LAMA4 laminin subunit alpha 4 JBrowse link 6 109,920,329 110,066,076 RGD:9068941
G MARCKS myristoylated alanine rich protein kinase C substrate JBrowse link 6 111,647,847 111,653,821 RGD:9068941
G NT5DC1 5'-nucleotidase domain containing 1 JBrowse link 6 113,903,473 114,051,784 RGD:9068941
G NUS1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link 6 115,486,422 115,521,317 RGD:9068941
G RFPL4B ret finger protein like 4B JBrowse link 6 109,950,749 110,162,597 RGD:9068941
G RFX6 regulatory factor X6 JBrowse link 6 114,686,132 114,741,072 RGD:9068941
G ROS1 ROS proto-oncogene 1, receptor tyrosine kinase JBrowse link 6 115,095,753 115,234,525 RGD:9068941
G RSPH4A radial spoke head component 4A JBrowse link 6 114,423,322 114,441,199 RGD:9068941
G RWDD1 RWD domain containing 1 JBrowse link 6 114,379,178 114,401,570 RGD:9068941
G TRAPPC3L trafficking protein particle complex 3 like JBrowse link 6 114,303,027 114,355,958 RGD:9068941
G TSPYL1 TSPY like 1 JBrowse link 6 114,079,317 114,082,540 RGD:9068941
G TSPYL4 TSPY like 4 JBrowse link 6 114,052,540 114,056,709 RGD:9068941
G USP9X ubiquitin specific peptidase 9 X-linked JBrowse link X 33,535,543 33,683,220 RGD:9068941
G VGLL2 vestigial like family member 2 JBrowse link 6 115,073,919 115,082,212 RGD:9068941
G ZUP1 zinc finger containing ubiquitin peptidase 1 JBrowse link 6 114,443,844 114,477,220 RGD:9068941
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DBH dopamine beta-hydroxylase JBrowse link 9 104,761,504 104,784,445 RGD:7240710
G HSPA5 heat shock protein family A (Hsp70) member 5 JBrowse link 9 96,351,645 96,356,761 RGD:9068941
neurocirculatory asthenia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 16 35,885,756 35,935,638 RGD:9068941
Orthostatic Hypotension term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ABCB1 ATP binding cassette subfamily B member 1 JBrowse link 7 79,497,536 79,706,277 RGD:9068941
G GNB3 G protein subunit beta 3 JBrowse link 12 6,971,854 6,979,214 RGD:9068941
G LOC100990650 guanine nucleotide-binding protein G(s) subunit alpha JBrowse link 20 55,190,607 55,262,245 RGD:9068941
G OPRD1 opioid receptor delta 1 JBrowse link 1 28,068,053 28,143,053 RGD:9068941
G OPRM1 opioid receptor mu 1 JBrowse link 6 151,827,323 151,937,658 RGD:9068941
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC100993774 cytochrome b561 JBrowse link 17 57,513,820 57,528,326 RGD:7240710
Orthostatic Intolerance term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 16 35,885,756 35,935,638 RGD:7240710
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NPPB natriuretic peptide B JBrowse link 1 10,621,416 10,622,960 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12677
    disease of anatomical entity 12213
      nervous system disease 9932
        Neurologic Manifestations 3724
          somatoform disorder 39
            Neurasthenia 0
            body dysmorphic disorder 28
            conversion disorder 0
            hypochondriasis 0
            neurocirculatory asthenia + 10
            pain disorder 0
            somatization disorder 0
Path 2
Term Annotations click to browse term
  disease 12677
    disease of anatomical entity 12213
      nervous system disease 9932
        central nervous system disease 8330
          brain disease 7669
            disease of mental health 5519
              somatoform disorder 39
                Neurasthenia 0
                body dysmorphic disorder 28
                conversion disorder 0
                hypochondriasis 0
                neurocirculatory asthenia + 10
                pain disorder 0
                somatization disorder 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.